Evidence map›Paper›PMID 24836453›Full record

ArticleAmerican journal of human genetics2014

Utilizing population controls in rare-variant case-parent association tests.

Yu Jiang, Glen A Satten, Yujun Han, Michael P Epstein, Erin L Heinzen, David B Goldstein, Andrew S Allen

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.0field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Yu JiangDepartment of Biostatistics and Bioinformatics, Duke University, Durham, NC 27710, USA.
Glen A SattenCenters for Disease Control and Prevention, Atlanta, GA 30333, USA.
Yujun HanCenter for Human Genome Variation, Duke University School of Medicine, Durham, NC 27708, USA.
Michael P EpsteinDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.
Erin L HeinzenCenter for Human Genome Variation, Duke University School of Medicine, Durham, NC 27708, USA.
David B GoldsteinCenter for Human Genome Variation, Duke University School of Medicine, Durham, NC 27708, USA.
Andrew S AllenDepartment of Biostatistics and Bioinformatics, Duke University, Durham, NC 27710, USA; Center for Human Genome Variation, Duke University School of Medicine, Durham, NC 27708, USA. Electronic address: andrew.s.allen@duke.edu.
Duke University · USCenters for Disease Control and Prevention · USEmory University · US

Funding

The Epilepsy Phenome/ Genome Project (EPGP)U01NS053998 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOWENSTEIN, DANIEL H · 2007 to 2013
$26.4M
3 of 7 Epi4K: Sequencing, Biostatistics & Bioinformatics CoreU01NS077303 · NINDS · DUKE UNIVERSITY · PI EICHLER, EVAN, GOLDSTEIN, DAVID B. · 2011 to 2018
$13.3M
2 of 7 EPI4K - Phenotyping Clinical Informatics Core U01NS077276 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOWENSTEIN, DANIEL H · 2011 to 2015
$3.1M
Enhanced Gene Identification in Complex Traits Using Kernel MachinesR01HG007508 · NHGRI · EMORY UNIVERSITY · PI EPSTEIN, MICHAEL PHILIP · 2013 to 2015
$1.0M
4 of 7: Epi4K: Epileptic Encephalopathies ProjectU01NS077364 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SHERR, ELLIOTT · 2011 to 2013
$827k
1 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes - Administrative CoreU01NS077274 · NINDS · DUKE UNIVERSITY · PI GOLDSTEIN, DAVID B. · 2011 to 2015
$776k
NHGRI NIH HHS HG007508NHGRI NIH HHS R01 HG007508NINDS NIH HHS NS053998NINDS NIH HHS NS077274NINDS NIH HHS NS077276NINDS NIH HHS NS077303NINDS NIH HHS U01 NS053998NINDS NIH HHS U01 NS077274NINDS NIH HHS U01 NS077276NINDS NIH HHS U01 NS077303NINDS NIH HHS U01 NS077364
6 · The paper itself

Abstract

There is great interest in detecting associations between human traits and rare genetic variation. To address the low power implicit in single-locus tests of rare genetic variants, many rare-variant association approaches attempt to accumulate information across a gene, often by taking linear combinations of single-locus contributions to a statistic. Using the right linear combination is key-an optimal test will up-weight true causal variants, down-weight neutral variants, and correctly assign the direction of effect for causal variants. Here, we propose a procedure that exploits data from population controls to estimate the linear combination to be used in an case-parent trio rare-variant association test. Specifically, we estimate the linear combination by comparing population control allele frequencies with allele frequencies in the parents of affected offspring. These estimates are then used to construct a rare-variant transmission disequilibrium test (rvTDT) in the case-parent data. Because the rvTDT is conditional on the parents' data, using parental data in estimating the linear combination does not affect the validity or asymptotic distribution of the rvTDT. By using simulation, we show that our new population-control-based rvTDT can dramatically improve power over rvTDTs that do not use population control information across a wide variety of genetic architectures. It also remains valid under population stratification. We apply the approach to a cohort of epileptic encephalopathy (EE) trios and find that dominant (or additive) inherited rare variants are unlikely to play a substantial role within EE genes previously identified through de novo mutation studies.

Indexed as

Computer SimulationControl GroupsEpilepsyGene FrequencyGenetic LociGenetic Predisposition to DiseaseGenetics, PopulationGenetic VariationGenome-Wide Association StudyGenotypeHumansLinkage DisequilibriumModels, GeneticParentsPhenotypeRare Diseases

Identifiers

PMID24836453
PMCPMC4121482
OpenAlexW2083259543

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.